Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:118342261-118342396 | Common:2; Rare:34 | ||||
chr10:118754919-118755288 | Common:1; Rare:122 | ||||
chr10:119080757-119080938 | Rare:73 | ||||
chr10:119165650-119165744 | Rare:43; Clinvar (benign):3 | ||||
chr10:119178786-119179021 | Common:3; Rare:80 | ||||
chr10:119651210-119651389 | Common:4; Rare:75; Clinvar (benign):2 | ||||
chr10:119725767-119726082 | Common:3; Rare:105 | ||||
chr10:119818510-119818762 | Rare:82 | ||||
chr10:119892540-119892779 | Common:3; Rare:90 | ||||
chr10:120456361-120456467 | Common:1; Rare:16 | ||||
chr10:120574881-120575148 | Common:3; Rare:50 | ||||
chr10:120851158-120851490 | Common:6; Rare:118 | ||||
chr10:121927899-121928208 | Common:2; Rare:93 | ||||
chr10:121928429-121928536 | Rare:28 | ||||
chr10:122879523-122879714 | Common:3; Rare:50 |